A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521595



Internal ID15448888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69089448..69109119hg38UCSC Ensembl
Innerchr11:68856916..68876587hg19UCSC Ensembl
Innerchr11:68613492..68633163hg18UCSC Ensembl
Innerchr11:68613492..68633163hg17UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3819672
hg1919672
hg1819672
hg1719672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698212
Samples
Known GenesTPCN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521595
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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